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HRID 15077作成日:2026年10月24日

Dimethylformamide → tert-butyl (3R)-3-(2-fluoroethoxy)pyrrolidine-1-carboxylate

https://huagongshe.com/ja/reaction/15077

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物2-Fluoroethyl p-ToluenesulfonateHCID 256019—
反応物tert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylateHCID 6544479—
溶媒Ethyl AcetateHCID 8857—
生成物tert-butyl (3R)-3-(2-fluoroethoxy)pyrrolidine-1-carboxylateHCID 8661489641%

反応手順

Sodium hydride (55% oiliness, 140 mg, 3.2 mmols) was added to DMF (5 mL) solution of tert-butyl (3R)-3-hydroxypyrrolidine-1-carboxylate (501.2 mg, 2.7 mmols) and stirred at room temperature for 30 minutes, followed by addition of 2-fluoroethyl p-toluenesulfonate (1.17 g, 5.4 mmols) and further 24 hours' stirring at the same temperature. Ethyl acetate was added to the reaction liquid which then was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the residue was purified on silica gel column chromatography (KP-Sil Sil FLASH 25+M, ethyl acetate:hexane=1:10→2:8) to provide the title compound (253 mg, 41%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732456B2
出典データセットuspto-grants-2010_06
ORD IDord-85ad0e45c6a6422c9234ea193065d75c
出典メモuspto-grants-2010_06